A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969368



Internal ID18604595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28447798..28449012hg38UCSC Ensembl
Innerchr6:28415575..28416789hg19UCSC Ensembl
Innerchr6:28523554..28524768hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381215
hg191215
hg181215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2399560, nssv2399564, nssv2399567, nssv2399563, nssv2399561, nssv2399559, nssv2399566, nssv2399562, nssv2399565, nssv2399568
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969368
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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